In the present investigation, fucoidan isolated from Nizamuddinia zanardinii was hydrolysed using 0.01 N HCl at boiling temperature for 10, 20, 40 and 60 min. Native and hydrolysed fucoidans contained a close chemical compositions, most importantly constituted of sulfates and uronic acids as well as fucose, galactose and mannose. Hydrolysis and cross-flow ultrafiltration produced fucoidan hydrolysates having different weight average molecular weights. The FH20 fucoidan was the most potent polysaccharide hydrolysate to stimulate NO-release from RAW264.7 macrophage cells. After cross-flow ultrafiltration of FH20, 100 < kDa fucoidan, polysaccharide with high branching degree consisting mainly of (1 → 2)-Fucp, (1 → 2,3)-Fucp, (1 → 3)-Galp, (1 → 2,3)-Galp, (1 → 2)-Manp and (1 → 3)-Manp residues, exerted the highest stimulation effect on RAW264.7 macrophage cells, secreting considerable NO, TNF-α, IL-1β, IL-6 and IL-12 proinflammatory mediators. Also, 100 < kDa fucoidan activated NK-92 cells to release TNF-α, INF-γ, granzyme-B, perforin, NKG2D and FasL. Both RAW264.7 and NK-92 cells were activated through NF-κB and MAPKs signalling pathways and the degree of stimulation capacity in fucoidan from N. zanardinii was in close correlation with the molecular weight.
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